@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_head
{
this:
np:hasAssertion
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_assertion
;
np:hasProvenance
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_provenance
;
np:hasPublicationInfo
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_assertion
a
np:Assertion
.
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_provenance
a
np:Provenance
.
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0265325
a
ncit:C7057
.
dgn-gda:DGN7fda027e86160589ba3e08987bd1232d
sio:SIO_000628
miriam-gene:5624
,
lld:C0265325
;
a
sio:SIO_001121
.
}
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_provenance
{
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_assertion
dcterms:description
"[To examine the possible involvement of mutations of the APC gene, which is responsible for familial adenomatous polyposis (FAP), in Turcot syndrome, we examined DNAs from TS patients for alterations in this gene by means of ribonuclease protection analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:7515658
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP518225.RAjRpsplBLlSxPnNXzKQB3mVNmxlOhZMawuo5EoNib0P4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}